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1                                Photoaffinity labeling of human protein geranylgeranyltransferase with
2                Here we report site-selective labeling of NDM-1 with 1,1,1-trifluoro-3-bromo acetone (
3                                   Retrograde labeling of the optic nerve with 1,1'-dioctadecyl-3,3,3'
4                                       Double labeling of cells with 12-(N-methyl)-N-[(7-nitrobenz-2-o
5 DeltaNK(IR)6.2/SUR1 channels exhibit reduced labeling of K(IR) with (125)I-azidoglibenclamide, implyi
6                                  Remarkably, labeling of 26S-associated USP14 with [(125)I]UbVS is in
7    Ing3A, but not PMA, blocked photoaffinity labeling of human P-gp with [(125)I]iodoaryazidoprazosin
8 hole cell transport assays and photoaffinity labeling of Pdr5p with [(125)I]iodoarylazidoprazosin in
9 entration-dependent manner the photoaffinity labeling of the multidrug transporter with 125I-iodoaryl
10                We performed in vivo isotopic labeling of Arabidopsis thaliana rosettes with (13)CO2 a
11                                              Labeling of the substrate with (13)C and (2)H was used t
12                                     Isotopic labeling of RNA with 13C and 15N has become a routine pr
13                         Direct photoaffinity labeling of microtubule protein with [14C]estramustine r
14 izoxin and paclitaxel decreased the covalent labeling of tubulin with [14C]estramustine in a dose-dep
15                              The progressive labeling of new peptides with (15)N and measuring the de
16 nance techniques depends on double or triple labeling of samples with (15)N, (13)C, and (2)H.
17 A9/G10.1 region is achieved by site-specific labeling of G10.1 with 15N guanine.
18                     We report the successful labeling of IL2 with (18)F for PET of activated T lympho
19                            Therefore, direct labeling of MSCs and MAPCs with (18)F-FDG is a suitable
20  as a general strategy for the site-specific labeling of other proteins with (18)F.
21                                              Labeling of PSMA tracers with (18)F offers numerous adva
22 ess an affinity for melanin, suggesting that labeling of such benzamides with (18)F could potentially
23 o be promising radioligands suitable for the labeling of SERT in vivo, with 18a providing a higher sp
24                            Immunofluorescent labeling of quail embryos with 1E12 and a MAb to smooth
25              The method is based on isotopic labeling of alpha-amino groups with 2, 4-dinitrofluorobe
26                                    Long term labeling of cells with [2-3H]mannose showed that the spe
27 l 4,5-bisphosphate, probed using equilibrium labeling of cells with [(3)H]myo-inositol.
28                                Photoaffinity labeling of CRABP-I with [(3)H]RA was light- and concent
29                                Photoaffinity labeling of porcine SR with [(3)H]azidodantrolene, a pho
30                                    Metabolic labeling of hCTPS2 with [(32)P]H(3)PO(4) demonstrated th
31                       We have used metabolic labeling of staphylococcal cultures with [(32)P]phosphor
32                                    Metabolic labeling of glial dynein with 32P followed by treatment
33                                    Metabolic labeling of the cultures with 32P revealed that NR2 subu
34 rylation, either in vivo following metabolic labeling of cells with [32P]orthophosphate or in vitro i
35 tation with anti-VSVG antibody after in vivo labeling of PS120/NHE3V cells with [32P]orthophosphate.
36                                              Labeling of roots with [32P]inorganic phosphate confirme
37  was established by demonstrating equivalent labeling of the protein with [32P]orthophosphate in the
38                                  Pulse-chase labeling of MRP1 with (35)S-methionine and (35)S-cystein
39 sults presented here indicate that metabolic labeling of cells with [(35)S]methionine under standard
40       Western blotting experiments and pulse labeling of infected cells with [(35)S]methionine demons
41 luR4 subunits were determined by pulse-chase labeling of cells with [35S]methionine.
42  by TGF-beta and CTGF was confirmed by pulse labeling of cells with [35S]methionine.
43                                    Metabolic labeling of cellular proteins with [35S]methionine after
44                                  Pulse-chase labeling of NEM-treated cells with [35S]methionine revea
45                            Kinetic metabolic labeling of cells with [3H]-leucine indicated that p19Ar
46                                        After labeling of cellular ACh pools with [3H]choline, potassi
47 ity of macrophages was assessed by metabolic labeling of M. tuberculosis with [3H]uracil.
48                                              Labeling of MC1 with [3H]NEM indicated that enhanced MT
49 smaller molecules was supported by metabolic labeling of mtDNA with [3H]thymidine during relaxed copy
50 echanistic studies showed that photoaffinity labeling of P-glycoprotein (Pgp) with [3H] azidopine was
51 almitoylation of the mutants was examined by labeling of the protein with [3H]-labeled palmitic acid.
52                                  Time course labeling of VV-infected cells with [3H]myristic acid rev
53                              Metabolic pulse-labeling of nascent RNA with 4'Thiouridine was used with
54 th bands are shifted to lower frequency upon labeling of the protein with [4-(13)C]aspartic acid.
55                                       Direct labeling of apotransferrin in situ with 45Ti was achieve
56         In both neonatal and adult mice, the labeling of dividing cells with 5-bromo-2'-deoxyuridine
57                                              Labeling of the iron with 54Fe confirms that the proxima
58                         We have used in vivo labeling of dividing cells with 6,6-(2)H(2)-glucose, com
59                    Using in vivo pulse-chase labeling of neutrophil DNA with 6,6-(2)H2-glucose, we fo
60                                              Labeling of this nanoparticle with (64)Cu yielded a high
61                                              Labeling of DOTANOC and DOTATATE with (68)Ga was standar
62                           However, metabolic labeling of A34 transgenic mice with (75)Se revealed tha
63                       In addition, metabolic labeling of MR cells with (75)Se revealed a loss of the
64 ighly modular and efficient strategy for the labeling of liposomal nanoparticles with (89)Zr.
65 ine-accessibility method that relies on mass-labeling of accessible SH groups with a large SH reagent
66 subunit specific antibody immunocytochemical labeling of cells with a neuronal morphology indicated t
67                         At embryonic day 18, labeling of cortical pyramidal cells with a yellow fluor
68 residues in a double-Cys mutant, followed by labeling of Cys148 with a thiol-reactive chelator that b
69                                     Affinity labeling of FAAH with a specific nucleophile reactive in
70                                    Metabolic labeling of glycans with a bioorthogonal chemical report
71 metry and size of VLPs are not influenced by labeling of HIV-1 Gag with a fluorescent protein.
72 etase (L274G) enables the cell-type-specific labeling of nascent proteins with a non-canonical amino-
73 lanilino)naphthalene-6-sulfonic acid (MIANS) labeling of permease with a single Cys residue in place
74                  We used in situ fluorescent labeling of proteins tagged with a short tetracysteine-c
75 the reaction irreversible, allowing complete labeling of proteins with a small excess of substrate an
76                      The long-term metabolic labeling of rats with a diet enriched in 15N did not res
77                     Using site-directed spin labeling of Ser(155)Cys with a nitroxide side chain, we
78 ach permits selective and efficient covalent labeling of small RNA duplexes with a variety of functio
79                          In vivo prospective labeling of Sox2-expressing cells with a Cre-lox system
80                                Intracellular labeling of streptococci with a nontoxic fluorescent dye
81  be identified on imaging by in vivo (99m)Tc labeling of the coronary thrombus with a compound that b
82                                Additionally, labeling of the systemin receptor with a photoaffinity a
83                                              Labeling of the unique cysteine with a sulfhydryl-reacti
84                                              Labeling of these polypeptides with a serine proteinase
85 ary epithelial cell membranes results in the labeling of two specific bands with a molecular weight o
86 C, we developed a new approach based on the "labeling" of tumors with a phospholipid "eat-me" signal,
87                                              Labeling of PICs with A3F-YFP, and to a lesser extent A3
88                    In this method, metabolic labeling of newly synthesized proteins with AHA endows t
89 de expansion and site-specific bioorthogonal labeling of rhodopsin with Alexa488 to enable, to our kn
90                           The method permits labeling of deacetylated residues with amine-reactive bi
91 states simultaneously through stable isotope labeling of cells with amino acids in cell culture (SILA
92 ee protein expression systems allow specific labeling of proteins with amino acids containing stable
93                                The metabolic labeling of cells with an alkynyl derivative of 20(S)-hy
94                                     Covalent labeling of M2 positions with an alcohol analog, a metha
95 ssess cytosolic delivery rely on fluorescent labeling of macromolecules with an "always on" reporter
96 fore, this review also addresses the in vivo labeling of organisms with an emphasis on plants.
97                                     Affinity labeling of the protease activity with an irreversible C
98                                   Successful labeling of proteins with Anl in several mammalian cell
99 rons but that in addition there is extensive labeling of glial cells associated with anterograde dege
100                   Indirect immunofluorescent labeling of aortic smooth muscle with anti-RyR antibodie
101                                              Labeling of synapses with anti-delta receptor antibody a
102                                       Immuno-labeling of these structures with anti-caveolin IgG conf
103                                     In vitro labeling of human blood cells with antibodies against ce
104                           Immunofluorescence labelings of differentiating myocytes with antibodies ag
105  conditions, we achieved fast, site-specific labeling of a protein with approximately 100% efficiency
106                                              Labeling of KatG with beta-methylene-deuterated tyrosine
107 it a low pK(a), and that the decrease in the labeling of cell lysate proteins with BIAM caused by pri
108                                        (32)P labeling of RNAs immunoprecipitated with BIG1 or nucleol
109                                     Specific labeling of biomolecules with biochemical and biophysica
110                                Intracellular labeling of astrocytes with biocytin revealed that CA1 a
111  hatchling chicks by using single and double labeling of fibers and terminals with biocytin conjugate
112                                              Labeling of natural products with biophysical probes has
113           This step was also devised to dual-labeling of PCR products with biotin and 6-FAM, which ar
114                     In studies examining the labeling of surface proteins with biotin in intact plate
115 purification method relies on the reversible labeling of thiol groups with biotin and exploitation of
116 m the spleens of immunized mice, followed by labeling of nontarget cells with biotinylated antibodies
117 the RBC anion transporter), as determined by labeling of RBC membranes with biotinylated ABA.
118                                              Labeling of the mice with BrdUrd demonstrated that, 7 da
119                                     Specific labeling of biomolecules with bright fluorophores is the
120                                              Labeling of cells with bromodeoxyuridine immediately pri
121                                    Metabolic labeling of live animals with bromodeoxyuridine at postn
122                                        Pulse-labeling of progenitors with bromodeoxyuridine showed th
123                                              Labeling of proliferating cells with bromodeoxyuridine d
124                          Ang II quantity and labeling of myocytes increased significantly with cardia
125 h a protein of interest allows site-specific labeling of the protein with CBT both in vitro and on th
126                                  Fluorescent labeling of budding yeast nucleoli with CDC14-GFP reveal
127                                           Co-labeling of Oc1 with cell cycle markers confirmed that O
128                                              Labeling of glomerular hybrid GBM with chain-specific an
129                                        Pulse labeling of endothelial cells with cholera toxin B subun
130      Purpose To determine whether endogenous labeling of macrophages with clinically applicable nanop
131  peptide termini labeling (IPTL) is based on labeling of both peptide termini with complementary isot
132 sidues in pterin-free NOS were identified by labeling of NOS with cysteine-directed reagents before a
133                                  Active site labeling of all prothrombin derivatives with D-Phe-Pro-A
134 y with clinically accepted in vivo metabolic labeling of tissue with deuterium to generate images of
135 es before isoelectric focusing, enabling the labeling of 2-3 samples with different dyes and electrop
136 cus pyogenes, is exploited for site-specific labeling of a single polypeptide with different labels a
137 tion nanoscopy, we imaged secondary antibody labeling of monoclonal AQP4-IgGs with differing epitope
138 pose, we marked these cells using retrograde labeling of fixed turtle retinas with DiI (1,1'-dioctade
139 eine labeling, this approach allows the dual labeling of proteins with distinct probes at two distinc
140               In each forebrain site, robust labeling of cells with distinguishable nuclei and short
141                         Rapid, site-specific labeling of proteins with diverse probes remains an outs
142  increased bradyzoite gene transcription and labeling of vacuoles with Dolichos biflorus lectin under
143                     Additionally, retrograde labeling of striatal neurons, along with double anterogr
144                                        Pulse-labeling of DNA with EdU and RNA with BrU and testing th
145                               In these mice, labeling of newborn GCs with eGFP lentiviruses revealed
146              Underpinning this method is the labeling of protein molecules with either iodine- or bro
147 (staph) is demonstrated by near-quantitative labeling of multiple protein substrates with excellent s
148                     In this study, metabolic labeling of bacteria with fatty acid chemical reporters
149                                Nevertheless, labeling of FDC reticula with FDC-M1 and anti-complement
150                                     In vitro labeling of autologous human leukocytes with FDG and (11
151                        Conclusion Endogenous labeling of macrophages with ferumoxytol enables noninva
152  48-50 h resulted in first- and second-order labeling of RV in combination with first-order labeling
153 in a fluorescent-activated cell sorter after labeling of K. lactis cells with fluorescein isothiocyan
154  assays using nitrocefin efflux and covalent labeling of Phe615Cys mutant AcrB with fluorescein-5-mal
155              We hypothesized that the double labeling of an adenovirus with fluorescent proteins woul
156                               Site-selective labeling of DTT with fluorescent dyes indicates that the
157 e first time a way for direct, site-specific labeling of proteins with fluorescent-dyes in live cells
158  layer of retinal cross-sections, retrograde labeling of retinal ganglion cells with fluorescent dye,
159 vity in response to sensory stimuli, and the labeling of single neurons with fluorescent proteins all
160                        This protocol entails labeling of the cellular compartment with fluorescent pr
161 ot rely on sampling and that uses retrograde labeling of RGCs with Fluorogold (Fluorochrome; Englewoo
162 ons in the SN, detected either by retrograde labeling of those cells with fluorogold or by tyrosine h
163 n or assembly within stressed cells, in situ labeling of sterically shielded cysteines with fluoropho
164 re dispensable for hair bundle integrity and labeling of hair cells with FM4-64, which was used as a
165                                Photoaffinity labeling of Rab4 with [gamma-(32)P]GTP-azidoanilide show
166                                Photoaffinity labeling of Rab5 with [gamma-(32)P]GTP-azidoanilide show
167  An optical signal was measured by secondary labeling of antigens with gold nanoparticles and their e
168          A general method of rigid, specific labeling of proteins with gold clusters has been devised
169        Inside the cell, we achieved specific labeling of cytoskeletal proteins with green and red flu
170                     Simultaneous multiplexed labeling of human keratinocytes with green QDs conjugate
171 tivity and specificity based on fluorescence labeling of DNA adducts combined with high-performance l
172  CD44 in breast cancer cells, we demonstrate labeling of fixed cells with high specificity that corre
173 o acid p-acetyl-L-phenylalanine for specific labeling of the protein with hydrazide derivatives of fl
174                              Although double-labeling of microglia with Iba1 and ED1 revealed numerou
175      Here we combine back-filling or genetic labeling of spinal interneurons with in situ staining fo
176 dihydrosphingosine, but it slightly affected labeling of sphingolipids with inositol.
177 l Tf IEF patterns were analyzed by metabolic labeling of fibroblasts with inverted question mark2-(3)
178                                    Moreover, labeling of this polypeptide correlated with irreversibl
179 s based on differential (12)C-/(13)C-isotope labeling of polyphenols through derivatization with isot
180                  Differential stable isotope labeling of the ClpPRS complex with iTRAQ revealed a fiv
181 with L-[methyl-3H]methionine and by in vitro labeling of cell proteins with L-[methyl-3H]S-adenosylme
182 n in NGF signaling was examined by metabolic labeling of PC12 cell proteins with L-[methyl-3H]methion
183  signaling pathways studies based on in vivo labeling of proteins with "light" (12C-labeled) or "heav
184                                    Metabolic labeling of cells with low-energy beta-emitting radioiso
185                      Lack of significant 13C labeling of glutamate was consistent with low respirator
186                                Photoaffinity labeling of HL-60 cells with LTC4-125I-ASA identified GA
187                  In addition, the Golgi-like labeling of neurons with many different colors provides
188 f-flight mass spectrometry combined with the labeling of specific ligands with mass tags enables dete
189                                     Covalent labeling of surface residues, combined with mass spectro
190                                              Labeling of intact rod photoreceptors with membrane mark
191                                Photoaffinity labeling of myofilament proteins with meta-Azi-propofol
192 been developed for the convenient N-terminal labeling of peptides with metal ion radionuclides of Bi(
193                                              Labeling of proteins with metallic radionuclides for use
194 al proteomics approach together with in vivo labeling of proteins with modified amino acids in mice t
195                                We report the labeling of IL2 with N-succinimidyl 4-(18)F-fluorobenzoa
196 euronal NOS (bNOS), combined with retrograde labeling of ganglion cells (GCs) with Neurobiotin (NB, a
197                                       Double labeling of sGC with neuronal nitric oxide synthase show
198                                       Double labeling of sGC with neuronal nitric oxide synthase show
199                     Cell-selective metabolic labeling of proteins with noncanonical amino acids enabl
200 structural analysis by combining fluorophore labeling of nucleic acids with novel quantitation algori
201 ine was observed with model amino acids, the labeling of protein amines with ONDs is fast enough to b
202                                       Double labeling of myocilin with other ECM components was perfo
203                                        Thus, labeling of tumors with phosphatidylserine is a promisin
204                                        Pulse labeling of ATMs with PKH26 assessed the recruitment rat
205                                              Labeling of recombinant proteins with polypeptide fusion
206 bunits NR1 and NR2B by combining anterograde labeling of thalamo-amygdaloid afferents with postembedd
207               We have performed 22 rounds of labeling of a single tissue with precise co-registration
208  maladaptive orienting to, interpreting, and labeling of potential threats, associated with prefronta
209  central nervous system (CNS) showed intense labeling of nuclear "gems," along with prominent nucleol
210 confirmed by loss of vasodilation to ACh and labeling of disrupted cells with propidium iodide), an a
211                       We show that selective labeling of proteins with protonated amino acids embedde
212 ) endocytic uptake of QDs and (ii) selective labeling of cell surface proteins with QDs conjugated to
213                                       Double labeling of gastric glands with rab3D and pepsinogen ant
214                               Direct ex vivo labeling of T lymphocytes with radioactive probes before
215 im of this study is to explore chelator-free labeling of LDH nanoparticles with radioisotopes for in
216                               Both metabolic labeling of calcineurin B with radiolabeled myristic aci
217                                    Also, the labeling of peptides with radiometals and applications o
218 ato-R CoRL reporter mice to induce permanent labeling of CoRL with red fluorescent protein variant td
219                                          The labeling of nucleotides and oligonucleotides with report
220  This region was identified by juxtacellular labeling of neurons with respiratory-related activity an
221 adhesion which was determined by fluorescent labeling of leukocytes with rhodamine 6G.
222                                 Coupling 32P labeling of intact mitochondria with SDS gel electrophor
223 lection of toxins on an antibody microarray, labeling of captured antigens with secondary biotinylate
224 lpha-subunit of the background construct and labeling of all five mutants with single cysteine residu
225                                              Labeling of bispecific antibodies with single-photon-emi
226                                          The labeling of proteins with small ubiquitin (Ub) and ubiqu
227                                     However, labeling of DNA with some fluorescent dyes, e.g., tetram
228  A method was developed using thiol-specific labeling of the ligand combined with subsequent immunoaf
229 t the catalytic site inhibited photoaffinity labeling of Pgp with substrate analogues, [125I]iodoaryl
230                                 Oxidation or labeling of hBCATm with sulfhydryl reagents results in e
231                                    Metabolic labeling of glycans with synthetic sugar analogs has eme
232 CT images were acquired 1 hour after in vivo labeling of RBCs with Tc-99m.
233                                       Double labeling of brain with terminal deoxynucleotidyl transfe
234 nzyme inactivation results from its covalent labeling of alpha with the sugar of F(2)CDP (one label/a
235 s or from the thymic monolayers, as shown by labeling of cells with the lipophilic membrane dye PKH26
236              Our method relies on asymmetric labeling of each subunit with the following scheme: spec
237 angement of TatA and TatB in intact cells by labeling of engineered cysteine residues with the membra
238                                     Although labeling of Escherichia coli with the chemical reporter
239                           In contrast to the labeling of every cell with the Cdc2 monoclonal antibody
240 ng a new method, that of [13C]carbon dioxide labeling of intact Arabidopsis plants with the subsequen
241 -based mitochondrial isolation procedure and labeling of mitochondria with the ratiometric fluorescen
242                              iPOND relies on labeling of nascent DNA with the nucleoside analog 5-eth
243                   Furthermore, photoaffinity labeling of P-gp with the substrate analogue [125I]iodoa
244 e of ATP hydrolysis by Pgp and photoaffinity labeling of Pgp with the substrate analogue [125I]iodoar
245                                   Retrograde labeling of premotor interneurons with the trans-synapti
246  with the widespread use of uniform isotopic labeling of proteins and RNA with the NMR-active isotope
247 suggest that the positive immunocytochemical labeling of Purkinje cells with the GluR2/3 antibody is
248                                       Immuno-labeling of skin equivalent sections with the anti-type
249                           Immunofluorescence labeling of the human tissue with the probe demonstrated
250 target Pcs and bioconjugation techniques for labeling of the oligonucleotides with the near-IR fluors
251 of human platelets showed significantly more labeling of the PM with the type III receptor antibodies
252 toreceptors were identified as cones by dual labeling of their inner segments with the lectin peanut
253                                       Double labeling of TSH4 with the ramosa2, branched silkless1 an
254 diffuse band of punctate labeling in CA1c to labeling of cell bodies along with their proximal dendri
255                      The degree of maleimide labeling of different residues correlated with their acc
256           The pharmacological specificity of labeling of residues, together with their locations in t
257 re was weak labeling of the OPL and stronger labeling of the IPL, with three distinct bands at the sa
258                                              Labeling of the particles with three different monoclona
259 otubule dynamics tend to rely on fluorescent labeling of tubulin, with tracking accuracy thereby limi
260                                    Metabolic labeling of DGA1 deletion strains with triglyceride prec
261  ganglion cells were quantified after double labeling of retinal tissue with TUNEL and Brn3a.
262  of this study is to quantify IHC images for labeling of ER status with two different crowdsourcing a
263                                       Double labeling of tissue with two different hair cell markers
264 the fatty acid synthetic pathway measured by labeling of six surgical specimens with [U-14C]acetate w
265                                          The labeling of proteins with ubiquitin/ubiquitin-like (Ubl)
266  fluorescence detection and the differential labeling of samples with up to four different fluorophor
267  fluoresceinated antibodies, indirect enzyme labeling of the bacteria with urease-labeled anti-fluore
268                                     Magnetic labeling of mammalian cells with use of ferumoxides and
269 xidase into a lumbar DRG resulted in intense labeling of IB4 axons, with very low background.
270 nd half-life were determined after metabolic labeling of CCS-/- fibroblasts transfected with wild-typ
271                                    Metabolic labeling of Cos7 cells transfected with wild type HHL1 c

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